Trials / Unknown
UnknownNCT01404637
Effects of Tamsulosin 0.4mg on Clinical Outcomes in Korean Men With Severe Symptomatic Benign Prostatic Hyperplasia (BPH)
The Effects of Tamsulosin 0.4mg on Clinical Outcomes in Korean Men With Severe Symptomatic BPH
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 150 (estimated)
- Sponsor
- Samsung Medical Center · Academic / Other
- Sex
- Male
- Age
- 45 Years – 80 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to compare the efficacy and safety of tamsulosin 0.4mg (Harnal® D. 0.2mg, 2T) with tamsulosin 0.2mg (Harnal® D 0.2mg, 1T) in patients with severe symptomatic benign prostatic hyperplasia as a first line therapy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Tamsulosin 0.4mg | Treatment: tamsulosin 0.2mg (2T) /day Posology: two 0.2 mg tablet to be taken after an evening meal. |
| DRUG | Tamsulosin 0.2mg | tamsulosin 0.2mg (1T) /day Posology: one tablet to be taken after an evening meal. |
Timeline
- Start date
- 2011-07-01
- Primary completion
- 2013-07-01
- Completion
- 2013-10-01
- First posted
- 2011-07-28
- Last updated
- 2011-08-02
Source: ClinicalTrials.gov record NCT01404637. Inclusion in this directory is not an endorsement.